Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Fentanyl Recalled by SCA Pharmaceuticals Due to Subpotency: Out-of-specification stability test result for low potency...

Date: November 20, 2020
Company: SCA Pharmaceuticals
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact SCA Pharmaceuticals directly.

Affected Products

Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205

Quantity: 4,843 syringes

Why Was This Recalled?

Subpotency: Out-of-specification stability test result for low potency was obtained.

Where Was This Sold?

This product was distributed to 2 states: LA, MO

Affected (2 states)Not affected

About SCA Pharmaceuticals

SCA Pharmaceuticals has 107 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report